A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893620



Internal ID18837754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2193473..2349298hg38UCSC Ensembl
Outerchr3:2193473..2349298hg38UCSC Ensembl
Innerchr3:2235157..2390982hg19UCSC Ensembl
Outerchr3:2235157..2390982hg19UCSC Ensembl
Innerchr3:2210157..2365982hg18UCSC Ensembl
Outerchr3:2210157..2365982hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38155826
hg19155826
hg18155826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790852
Samples
Known GenesCNTN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893620
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer